• Je něco špatně v tomto záznamu ?

"Clickable" and Antifouling Block Copolymer Brushes as a Versatile Platform for Peptide-Specific Cell Attachment

R. Poręba, A. de Los Santos Pereira, R. Pola, S. Jiang, O. Pop-Georgievski, Z. Sedláková, H. Schönherr

. 2020 ; 20 (4) : e1900354. [pub] 20200219

Jazyk angličtina Země Německo

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc21020661

To tailor cell-surface interactions, precise and controlled attachment of cell-adhesive motifs is required, while any background non-specific cell and protein adhesion has to be blocked effectively. Herein, a versatile and highly reproducible antifouling surface modification based on "clickable" groups and hierarchically structured diblock copolymer brushes for the controlled attachment of cells is reported. The polymer brush architecture combines an antifouling bottom block of poly(2-hydroxyethyl methacrylate) poly(HEMA) and an ultrathin azide-bearing top block, which can participate in well-established "click" reactions including the highly selective copper-catalyzed alkyne-azide cycloaddition (CuAAC) reaction under mild conditions. This straightforward approach allows the rapid conjugation of a cell-adhesive, alkyne-bearing cyclic RGD peptide motif, enabling subsequent specific attachment of NIH 3T3 fibroblasts, their extensive proliferation and confluent cell sheet formation after 48 h of incubation. The generally applicable strategy presented in this report can be employed for surface functionalization with diverse alkyne-bearing biological moieties via CuAAC or copper-free alkyne-azide cycloaddition protocols, making it a versatile functionalization approach and a promising tool for tissue engineering, biomaterial implant design, and other applications that require surfaces supporting highly specific cell attachment.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc21020661
003      
CZ-PrNML
005      
20210830102257.0
007      
ta
008      
210728s2020 gw f 000 0|eng||
009      
AR
024    7_
$a 10.1002/mabi.201900354 $2 doi
035    __
$a (PubMed)32077245
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a gw
100    1_
$a Poręba, Rafał $u Institute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovsky sq. 2, Prague, 162 06, Czech Republic
245    10
$a "Clickable" and Antifouling Block Copolymer Brushes as a Versatile Platform for Peptide-Specific Cell Attachment / $c R. Poręba, A. de Los Santos Pereira, R. Pola, S. Jiang, O. Pop-Georgievski, Z. Sedláková, H. Schönherr
520    9_
$a To tailor cell-surface interactions, precise and controlled attachment of cell-adhesive motifs is required, while any background non-specific cell and protein adhesion has to be blocked effectively. Herein, a versatile and highly reproducible antifouling surface modification based on "clickable" groups and hierarchically structured diblock copolymer brushes for the controlled attachment of cells is reported. The polymer brush architecture combines an antifouling bottom block of poly(2-hydroxyethyl methacrylate) poly(HEMA) and an ultrathin azide-bearing top block, which can participate in well-established "click" reactions including the highly selective copper-catalyzed alkyne-azide cycloaddition (CuAAC) reaction under mild conditions. This straightforward approach allows the rapid conjugation of a cell-adhesive, alkyne-bearing cyclic RGD peptide motif, enabling subsequent specific attachment of NIH 3T3 fibroblasts, their extensive proliferation and confluent cell sheet formation after 48 h of incubation. The generally applicable strategy presented in this report can be employed for surface functionalization with diverse alkyne-bearing biological moieties via CuAAC or copper-free alkyne-azide cycloaddition protocols, making it a versatile functionalization approach and a promising tool for tissue engineering, biomaterial implant design, and other applications that require surfaces supporting highly specific cell attachment.
650    _2
$a alkyny $x chemie $x farmakologie $7 D000480
650    _2
$a zvířata $7 D000818
650    _2
$a antiinfekční látky $x chemická syntéza $x farmakologie $7 D000890
650    _2
$a azidy $x chemie $x farmakologie $7 D001386
650    _2
$a biokompatibilní materiály $x chemická syntéza $x farmakologie $7 D001672
650    _2
$a katalýza $7 D002384
650    _2
$a proliferace buněk $x účinky léků $7 D049109
650    _2
$a syntetická chemie okamžité shody $7 D057930
650    _2
$a cykloadiční reakce $7 D061565
650    _2
$a myši $7 D051379
650    _2
$a buňky NIH 3T3 $7 D041681
650    _2
$a oligopeptidy $x chemie $7 D009842
650    _2
$a polyhydroxyethylmethakrylát $x chemie $7 D011102
650    _2
$a tkáňové inženýrství $7 D023822
650    12
$a tkáňové podpůrné struktury $7 D054457
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a de Los Santos Pereira, Andres $u Institute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovsky sq. 2, Prague, 162 06, Czech Republic
700    1_
$a Pola, Robert $u Institute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovsky sq. 2, Prague, 162 06, Czech Republic
700    1_
$a Jiang, Siyu $u Physical Chemistry I and Research Center of Micro and Nanochemistry and Engineering (Cµ), Department of Chemistry and Biology, University of Siegen, Adolf-Reichwein-Str. 2, 57076, Siegen, Germany
700    1_
$a Pop-Georgievski, Ognen $u Institute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovsky sq. 2, Prague, 162 06, Czech Republic
700    1_
$a Sedláková, Zdeňka $u Institute of Macromolecular Chemistry, Czech Academy of Sciences, Heyrovsky sq. 2, Prague, 162 06, Czech Republic
700    1_
$a Schönherr, Holger $u Physical Chemistry I and Research Center of Micro and Nanochemistry and Engineering (Cµ), Department of Chemistry and Biology, University of Siegen, Adolf-Reichwein-Str. 2, 57076, Siegen, Germany
773    0_
$w MED00006593 $t Macromolecular bioscience $x 1616-5195 $g Roč. 20, č. 4 (2020), s. e1900354
856    41
$u https://pubmed.ncbi.nlm.nih.gov/32077245 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y p $z 0
990    __
$a 20210728 $b ABA008
991    __
$a 20210830102257 $b ABA008
999    __
$a ok $b bmc $g 1691271 $s 1141107
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2020 $b 20 $c 4 $d e1900354 $e 20200219 $i 1616-5195 $m Macromolecular bioscience $n Macromol Biosci $x MED00006593
LZP    __
$a Pubmed-20210728

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...